WO2003011871A2 - Intermediates in cephalosporin production - Google Patents
Intermediates in cephalosporin production Download PDFInfo
- Publication number
- WO2003011871A2 WO2003011871A2 PCT/EP2002/008554 EP0208554W WO03011871A2 WO 2003011871 A2 WO2003011871 A2 WO 2003011871A2 EP 0208554 W EP0208554 W EP 0208554W WO 03011871 A2 WO03011871 A2 WO 03011871A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cefprozil
- paca
- salt
- amidine
- group
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
Definitions
- the present invention relates to intermediates in cephalosporin production.
- Cefprozil [6R-[6 ⁇ ,7 ⁇ (R*)]]-7-[[amino(4-hydroxyphenyl)acetyl]amino]-8-oxo-3-(1-propenyl)-3- thia-1 -azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid e.g. in the form of a monohydrate (see e.g. The Merck Index, 12 th edition, item 1992), is a broadly used cephalosporin antibiotic.
- cefprozil e.g. in the form of a monohydrate, e.g. in pure form.
- the present invention provides a process for the production of cefprozil, e.g. in the form of a solvate, e.g. hydrate, such as a monohydrate, comprising the steps A1 ) reacting PACA of formula
- X + is a group of formula
- Y is a group of formula -NR 3 R 4 and a1)
- R to R 5 are the same or different and are independently of each other hydrogen, alkyl or aryl; or a2) two of the substituents R 1( R 2 and R 5 , and/or R 3 and R 4 together form a -(CH 2 ) 2 - or -(CH 2 )3- group; and the other substituents R ⁇ to R 5 are as defined above; or b) Y forms together with R 2 a -(CH 2 ) 3 - or -(CH 2 ) 5 - group, and R ⁇ and R 5 together form a -(CH 2 ) 3 - group, with a mixed carboxylic acid anhydride of an ⁇ -amino-p-hydroxyphenylacetic acid, and B1) isolating ceprozil from the reaction mixture obtained in step A1); and optionally C1) converting cefprozil isolated in step B1) into ceprozil in the form of a mono
- the present invention provides a process for the production of cefprozil, e.g. in the form of a solvate, e.g. N,N-dimethylformamide (DMF) solvate (e.g. cefprozil x1.5 DMF) or hydrate, e.g. monohydrate, which comprises the steps
- step A2 reacting a mixed carboxylic acid anhydride obtainable in step A2) with PACA in the form of a salt with an amidine, e.g. a compound of formula I wherien X + is as defined above,
- cefprozil isolating cefprozil, e.g. in the form of a solvate, e.g. N,N-dimethylformamide solvate, e.g. in crystalline form; obtained in step B2), and optionally
- step D2) converting cefprozil obtained in step C2), e.g. in the form of an N,N-dimethylformamide solvate; into cefprozil in the form of a hydrate; e.g. a monohydrate.
- a process according to the present invention may be carried out as appropriate, e.g. according to, e.g. analogously, to a method as conventional, and is preferably carried out as follows:
- Step A1), or step B2), respectively, is an acylation reaction with a mixed carboxylic acid anhydride.
- An appropriate mixed carboxylic acid anhydride is preferably provided according to step
- A2) i.e. by acylating, e.g. reacting, an N-vinyl substituted ⁇ -amino-p-hydroxyphenylacetic acid, with an appropriate acylating agent.
- the N-substituted vinyl ⁇ -amino- p-hydroxyphenylacetic acid may be used in free form or in the form of a salt, e.g. including a Dane salt, such as sodium or potassium D-N-(1-methoxycarbonylpropen-2-yl)- ⁇ -amino-p- hydroxyphenylacetate, or sodium or potassium D-N-(1 -ethoxycarbonyl-propen-2-yl)- ⁇ - amino-p-hydroxyphenylacetate.
- acylating agents include aliphatic, alicyclic, or aromatic acids, e.g. including alkanoic acids, such as chloroformic acid, pivalic acid, 2- ethylhexanoic acid, benzoic acid, e.g. in a reactive form.
- a reactive form includes acid halogenides, e.g. chlorides, e.g. including pivaloyl chloride, 2-ethyl-hexanoyl chloride, benzoyl chloride and esters, e.g. chloroformic acid alkyl esters, such as ethyl chloroformate.
- a small amount of a free C -C 9 acid may be present, e.g.
- an alkanoic acid such as pivalic acid or 2-ethylhexanoic acid
- an aromatic acid e.g. benzoic acid, preferably 2- ethylhexanoic acid or pivalic acid, e.g. which may catalyze the mixed carboxylic acid anhydride formation.
- the side chain of said free carboxylic acid may be the same or different to that of the acylating agent and is preferably the same.
- Appropriate solvents in step A2) include halogenated hydrocarbons e.g dichloromethane or acetic acid (C ⁇ . 4 )alkylesters such as butylacetate or isopropylacetate.
- a co-solvent may be present which may improve or activate the reaction of above Dane salts with the acylating agent, such as organic amides, e.g. in the form of N-subsituted amides, e.g. including formamide, acetamides, N-mono or N,N-dimethyl amides, such as N,N-dimethyl formamide (DMF), N- methylacetamide, N,N-dimethylacetamide; pyrrolidines, such as N-methylpyrrolidines; ureas, e.g. tetramethylurea, branched chain alkyl alcohols, such as isopropanol; preferably DMF.
- a base e.g.
- a tertiary amine base may be present as a catalyst in step A2).
- a preferred base includes pyridines, for example a picoline, e.g. 3- or 4-picoline, or a lutidine.
- the formation of the mixed carboxylic acid anhydride in step A2) may be effected at temperatures as appropriate, e.g. including temperatures from -50° to 50°C, preferably from -40°C to 0°C.
- a solution or a suspension of a mixed carboxylic acid anhydride may be obtained which may be used further, e.g. in step A1) or B2), as such, e.g. without isolation of the mixed carboxylic acid anhydride, e.g. which solution or a suspension may be stored, e.g. at appropriate temperatures, e.g. including temperatures from (ca.) -60°C to -20°C.
- Step A1 is an acylation reaction of the amine group of a PACA- amidine with a mixed carboxylic acid anhydride, e.g. obtainable according to step A2).
- PACA in the form of a salt with an amidine, e.g. a compound of formula I, wherein X + is as defined above, is novel.
- the present invention provides PACA of formula
- a salt with an amidine e.g. a compound of formula I as defined above wherein X + is as defined above, e.g. in the form of an acid addition salt or in the form of a solvate of a compound of formula I or in the form of a solvate of an acid addition salt of a compound of formula I.
- the present invention provides the use of a compound according to the present invention, e.g. as an intermediate, in the production of cefprozil.
- PACA in the form of a salt(s) with an amidine according to the present invention is hereinafter designated as "PACA-amidine(s)".
- PACA-amidines may exist in free form, in the form of a salt, in the form of a solvate and in the form of a salt and a solvate.
- PACA-amidines in free form may be converted into PACA- amidines in the form of a salt and vice versa.
- PACA-amidines in the form of a solvate or in the form of a salt and a solvate may be converted into PACA-amidines in unsolvated form or PACA-amidines in the form of a salt in unsolvated form and vice versa.
- PACA-amidines are e.g.
- PACA-amidines may be stable despite the high basicity of the corresponding bases, e.g.
- Appropriate guanidine salts include e.g. compounds of formula II, wherein Y denotes a group of formula -NR 3 R 4 wherein R 3 and R 4 are as -defined above.
- any carbon atom containing group preferably may contain up to 20 carbon atoms.
- Aryl includes phenyl, naphthyl. Any group may be unsubstituted or substituted, e.g. substituted as appropriate, e.g. according, e.g. analogously, as conventional in organic chemistry, e.g. ⁇ -lactam chemistry, such as cephalosporin chemistry.
- a solvent includes a solvent mixture (system) of individual solvents, e.g. as correspondingly indicated.
- Y is a group of formula -NR 3 R 4 and R ⁇ to R 5 are independently of each other hydrogen, unsubstituted alkyl or alkyl substituted by a phenyl group, for example benzyl, or unsubstituted aryl; preferably Ri, R 2 , R 3 and R 4 are (C 1-4 )alkyl and R 5 is hydrogen; or Y together with R 2 form a -(CH 2 ) 3 - or -(CH 2 ) 5 - group, and R, and R 5 together form a -(CH 2 ) 3 - group.
- Preferred PACA-amidines include PACA in the form of a salt with tetramethylguanidine (TMG), 1 ,8-diazabicyclo[5.4.0]undec-7-ene (DBU), 1 ,5- diazabicyclo[4.3.0]non-5-ene (DBN).
- TMG tetramethylguanidine
- DBU 1 ,8-diazabicyclo[5.4.0]undec-7-ene
- DBN diazabicyclo[4.3.0]non-5-ene
- PACA-amidine salt is a salt formation process which may be carried out as appropriate, and is preferably carried out as follows:
- PACA may be suspended in an appropriate solvent and an amidine is added.
- An appropriate solvent system is described below for providing a solution of a PACA-amidine.
- a solution may be obtained, e.g. if PACA is in the form of a salt with a guanidine which guanidine is in the form of a free base.
- the ratio of PACA and an amidine is not critical. E.g. per equivalent PACA 1 to 2, e.g. 1 to 1.5, preferably 1 to 1.2 equivalents of an amidine may be used.
- a PACA-amidine may be isolated in the form of a solid, e.g. an amorphous powder, foam, e.g.
- solvent may be evaporated off and the evaporation residue may be treated with an anti-solvent.
- An anti-solvent is a solvent wherein a PACA- amidine is less soluble than in a solvent, e.g. including ethers, e.g. tert. butyl-methylether, diethylether, or hydrocarbons, e.g. hexane.
- a PACA-amidine may be isolated as appropriate, e.g by solvent decantation or filtration.
- An appropriate solvent system for providing a solution of a PACA-amidine and for providing PACA-amidines includes e.g. halogenated hydrocarbons, preferably dichloromethane, alkanols, e.g.
- (C ⁇ - 4 ) alkanols such as ethanol, butanol, isopropanol, preferably a (C 3 . 4 )alkanol, such as butanol, for example n-butanol, iso-butanol, tert.-butanol or sec- butanol, or isopropanol, e.g. isopropanol; optionally in combination with a solvent as described above in step A2).
- water may be present.
- the present invention provides a process for the production of PACA in the form of a salt with an amidine comprising suspending PACA of formula III in an appropriate solvent, adding an amidine and isolating PACA in the form of a salt with an amidine.
- a solution of a PACA- amidine e.g. obtainable as described above, may be reacted with, e.g. may be added to, a reaction mixture comprising a mixed carboxylic acid anhydride, e.g. obtainable according to step A2).
- a reaction mixture comprising a mixed carboxylic acid anhydride, e.g. obtainable according to step A2).
- a small amount of water may be present in the solvent (system).
- a small amount of a (C . 9 )alkanoic acid e.g. including 2-ethylhexanoic acid, may be added to a mixture of a PACA-amidine and solvent (system).
- Appropriate reaction temperatures include e.g.
- Cefprozil e.g. in a protected form, may be obtained.
- Cefprozil in a protected form e.g. includes cefprozil, wherein the amine group of the glycyl group attached to the amine group in position 7 of the ring structure, is protected by a substituted vinyl group, e.g. according to a Dane salt used in the production of a mixed anhydride, e.g. as described above in step A2.
- ceprozil is obtained in a protected form cefprozil may be deproteced, e.g. a substituted vinyl group may be split off as appropriate, e.g. by hydrolysis in aqueous acid.
- Cefprozil may be obtained and may be isolated.
- Step B1), or C2), respectively, i.e. the isolation of cefprozil may be carried out as appropriate and is preferably carried out as follows:
- the reaction mixture obtained in step A1 ) or B2), respectively, may be worked up as appropriate and cefprozil may be isolated as appropriate, e.g. according, e.g. analogously, to a method as conventional.
- Cefprozil is preferably isolated in the form of a solvate, e.g. in the form of an N,N-dimethylformamide solvate (1/1.5), e.g.
- cefprozil in the form of a DMF-solvate e.g. in crystalline form, is e.g. described in US 4,694,079 which is introduced herein by reference.
- Step C1 ) or D2), respectively, i.e. conversion of cefprozil, e.g. in the form of a DMF-solvate, into cefprozil in the form of a hydrate, e.g. monohydrate may be carried out as appropriate and is preferably carried out as follows:
- Cefprozil e.g. in the form of an DMF-solvate (e.g. 1/1.5) may be mixed with water and an inorganic acid, e.g. hydrochloric acid; e.g. dissolution of cefprozil may be facilitated by addition of said inorganic acid.
- an inorganic acid e.g. hydrochloric acid
- dissolution of cefprozil may be facilitated by addition of said inorganic acid.
- cefprozil in the form of a hydrate e.g. a monohydrate may be crystallized by addition of an inorganic base, e.g. including sodium hydroxide or aqueous ammonia to adjust a pH which is around the isoelectric point of cefprozil, e.g. at appropriate temperatures, e.g. including temperatures of room temperature or above, e.g.
- cefprozil e.g. in the form of an DMF-solvate
- cefprozil in the form of a monohydrate by heating a solution or suspension in water at elevated temperates, e.g. including temperatures of 30°C to 60°C.
- Ceprozil in the form of a hydrate, e.g. monohydrate, e.g. in crystalline form may be isolated from the reaction mixture as appropriate, e.g. by filtration, centrifugation.
- a suspension of 148 ml of CH 2 CI 2 and 20.77 g of PACA is cooled to -10° and 11.43 ml of TMG are added.
- the suspension obtained is warmed up and a solution is obtained.
- the solution obtained is cooled to -50°.
- the solution obtained in step 1 b) is added to the suspension obtained in step 1 a) at a rate that the temperature does not exceed -40° and the mixture obtained is stirred at -45° for ca. 1 hour and at -35° for ca. 2 hours.
- Cefprozil wherein the amine group of the glycyl group attached to the amine group in position 7 of the cephalosporin ring structure is protected by a 1 -methoxycarbonylpropen-2-yl group is obtained. d) Cefprozil in the form of a DMF-solvate
- step 1c) The mixture obtained in step 1c) is added to a mixture of 81 ml of ice water and 18 ml of concentrated HCI and the mixture obtained is stirred. Two phases obtained are separated. To the aqueous layer obtained 180 ml of DMF are added and the pH of the mixture obtained is adjusted with 25% aqueous ammonia to 2.5 at a temperature of ca. 30°. To the mixture obtained 44 ml of DMF are added and the pH is adjusted to 4.2 with 25% aqueous ammonia. To the mixture obtained seed crystalls of a DMF-solvate, i.e. cefprozil x(1/1.5) DMF solvate are added.
- a DMF-solvate i.e. cefprozil x(1/1.5) DMF solvate
- Cefprozil in the form of a cefprozil x(1/1.5) DMF solvate crystallizes. The pH of the suspension obtained is adjusted to 6.8 and the suspension is allowed to stand at 30°. Cefprozil in the form of a cefprozil x(1/1.5) DMF solvate in crystalline form is filtrated off, washed and dried. e) Cefprozil in the form of a monohydrate
- PACA in the form of a salt with TMG is obtained in the form of an amorphous powder.
- PACA in the form of a salt with DBU is obtained in the form of an amorphous powder.
- PACA in the form of a salt with DBN in the form of an amorphous powder is obtained.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Cephalosporin Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP02791486A EP1414827A2 (en) | 2001-08-01 | 2002-07-31 | Intermediates in cephalosporin production |
US10/485,420 US7355041B2 (en) | 2001-08-01 | 2002-07-31 | Intermediates in cefprozil production |
CA002454078A CA2454078A1 (en) | 2001-08-01 | 2002-07-31 | Intermediates in cephalosporin production |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0118764.0A GB0118764D0 (en) | 2001-08-01 | 2001-08-01 | Organic compounds |
GB0118764.0 | 2001-08-01 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2003011871A2 true WO2003011871A2 (en) | 2003-02-13 |
WO2003011871A3 WO2003011871A3 (en) | 2003-12-04 |
Family
ID=9919622
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2002/008554 WO2003011871A2 (en) | 2001-08-01 | 2002-07-31 | Intermediates in cephalosporin production |
Country Status (6)
Country | Link |
---|---|
US (1) | US7355041B2 (en) |
EP (1) | EP1414827A2 (en) |
CA (1) | CA2454078A1 (en) |
GB (1) | GB0118764D0 (en) |
TW (1) | TWI250982B (en) |
WO (1) | WO2003011871A2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004110399A2 (en) * | 2003-06-19 | 2004-12-23 | Ranbaxy Laboratories Limited | Solvates of cefprozil |
WO2005042544A1 (en) * | 2003-10-30 | 2005-05-12 | Cj Corporation | Processes for the preparation of cephalosporin derivatives |
WO2006048887A1 (en) * | 2004-11-01 | 2006-05-11 | Hetero Drugs Limited | A novel process for preparation of cefprozil intermediate |
US7230097B2 (en) | 2003-03-10 | 2007-06-12 | Lupin Ltd. | Process for preparation of 7-[α-Amino (4-hydroxyphenyl) acetamido]-3-substituted-3-cephem-4-carboxylic acid |
CN102408438A (en) * | 2010-09-26 | 2012-04-11 | 石药集团中奇制药技术(石家庄)有限公司 | Preparation method of cefprozil monohydrate |
CN102443013A (en) * | 2010-10-10 | 2012-05-09 | 石药集团中奇制药技术(石家庄)有限公司 | Method for preparing cefprozil dimethyl formamide solvate |
CN103524533A (en) * | 2013-10-10 | 2014-01-22 | 珠海金鸿药业股份有限公司 | Cefprozil compound, and dispersible tablets, dry suspension and preparation method thereof |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7662955B2 (en) * | 2003-03-20 | 2010-02-16 | Orchid Chemicals And Pharmaceuticals Ltd. | Process for the preparation of cefoxitin |
WO2006103686A1 (en) * | 2005-03-29 | 2006-10-05 | Hetero Drugs Limited | An improved process for the preparation of cefixime |
Citations (3)
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US4619925A (en) * | 1985-11-08 | 1986-10-28 | Bristol-Myers Company | 3-Propenyl cephalosporin derivatives |
WO1998004732A1 (en) * | 1996-07-26 | 1998-02-05 | Bristol-Myers Squibb Company | SYNTHESIS OF β-LACTAM ANTIBACTERIALS USING SOLUBLE SIDE CHAIN ESTERS AND ENZYME ACYLASE |
WO2001030783A1 (en) * | 1999-10-27 | 2001-05-03 | Dsm N.V. | PROCESS FOR THE PREPARATION OF A β-LACTAM ANTIBIOTIC |
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ES8102578A1 (en) | 1980-02-20 | 1981-02-16 | Gema Sa | Process for the preparation of 7-(D(-)-alpha-amino-p-hydroxyphenylacetamido)desacetoxycephalosporanic acid |
ES8505362A1 (en) | 1983-05-26 | 1985-06-01 | Gema Sa | Salts of amino-beta-lactamic acids and process for the preparation thereof. |
GB9115203D0 (en) | 1991-07-15 | 1991-08-28 | Biochemie Gmbh | Improvements in or relating to beta lactam production |
WO1993016084A1 (en) * | 1992-02-05 | 1993-08-19 | Biochemie Gesellschaft M.B.H. | Process for the purification of a 3-cephem-4-carboxylic acid derivative |
US5908929A (en) | 1996-12-05 | 1999-06-01 | Vitara Chemicals Limited | Process for the manufacture of the antibiotic 7-(D-α-amino-α-phenylacetamido)-3-methyl-3-cephem-4-carboxylic acid (cephalexin) and pharmaceutically acceptable salts thereof |
US6903211B2 (en) * | 2002-10-30 | 2005-06-07 | Orchid Chemicals & Pharmaceuticals Limited | Process for the preparation of 3-propenyl cephalosporin DMF solvate |
US7230097B2 (en) * | 2003-03-10 | 2007-06-12 | Lupin Ltd. | Process for preparation of 7-[α-Amino (4-hydroxyphenyl) acetamido]-3-substituted-3-cephem-4-carboxylic acid |
-
2001
- 2001-08-01 GB GBGB0118764.0A patent/GB0118764D0/en not_active Ceased
-
2002
- 2002-07-30 TW TW091117039A patent/TWI250982B/en not_active IP Right Cessation
- 2002-07-31 EP EP02791486A patent/EP1414827A2/en not_active Withdrawn
- 2002-07-31 WO PCT/EP2002/008554 patent/WO2003011871A2/en not_active Application Discontinuation
- 2002-07-31 CA CA002454078A patent/CA2454078A1/en not_active Abandoned
- 2002-07-31 US US10/485,420 patent/US7355041B2/en not_active Expired - Fee Related
Patent Citations (3)
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US4619925A (en) * | 1985-11-08 | 1986-10-28 | Bristol-Myers Company | 3-Propenyl cephalosporin derivatives |
WO1998004732A1 (en) * | 1996-07-26 | 1998-02-05 | Bristol-Myers Squibb Company | SYNTHESIS OF β-LACTAM ANTIBACTERIALS USING SOLUBLE SIDE CHAIN ESTERS AND ENZYME ACYLASE |
WO2001030783A1 (en) * | 1999-10-27 | 2001-05-03 | Dsm N.V. | PROCESS FOR THE PREPARATION OF A β-LACTAM ANTIBIOTIC |
Non-Patent Citations (1)
Title |
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Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7230097B2 (en) | 2003-03-10 | 2007-06-12 | Lupin Ltd. | Process for preparation of 7-[α-Amino (4-hydroxyphenyl) acetamido]-3-substituted-3-cephem-4-carboxylic acid |
US7427692B2 (en) | 2003-03-10 | 2008-09-23 | Lupin Ltd. | Process for preparation of 7-[α-amino (4-hydroxyphenyl) acetamido]-3-substituted-3-cephem-4-carboxylic acid |
WO2004110399A3 (en) * | 2003-06-19 | 2005-02-17 | Ranbaxy Lab Ltd | Solvates of cefprozil |
WO2004110399A2 (en) * | 2003-06-19 | 2004-12-23 | Ranbaxy Laboratories Limited | Solvates of cefprozil |
US7622577B2 (en) | 2003-10-30 | 2009-11-24 | Cj Cheiljedang Corporation | Processes for the preparation of cephalosporin derivatives |
EP1678187A1 (en) * | 2003-10-30 | 2006-07-12 | CJ Corporation | Processes for the preparation of cephalosporin derivatives |
EP1678187A4 (en) * | 2003-10-30 | 2007-06-13 | Cj Corp | Processes for the preparation of cephalosporin derivatives |
WO2005042544A1 (en) * | 2003-10-30 | 2005-05-12 | Cj Corporation | Processes for the preparation of cephalosporin derivatives |
WO2006048887A1 (en) * | 2004-11-01 | 2006-05-11 | Hetero Drugs Limited | A novel process for preparation of cefprozil intermediate |
US7629482B2 (en) | 2004-11-01 | 2009-12-08 | Hetero Drugs Limited | Process for preparation of cefprozil intermediate |
EP2213676A1 (en) * | 2004-11-01 | 2010-08-04 | Hetero Drugs Limited | A Novel process for preparation of cefprozil |
CN102408438A (en) * | 2010-09-26 | 2012-04-11 | 石药集团中奇制药技术(石家庄)有限公司 | Preparation method of cefprozil monohydrate |
CN102408438B (en) * | 2010-09-26 | 2015-01-07 | 石药集团中奇制药技术(石家庄)有限公司 | Preparation method of cefprozil monohydrate |
CN102443013A (en) * | 2010-10-10 | 2012-05-09 | 石药集团中奇制药技术(石家庄)有限公司 | Method for preparing cefprozil dimethyl formamide solvate |
CN102443013B (en) * | 2010-10-10 | 2014-09-17 | 石药集团中奇制药技术(石家庄)有限公司 | Method for preparing cefprozil dimethyl formamide solvate |
CN103524533A (en) * | 2013-10-10 | 2014-01-22 | 珠海金鸿药业股份有限公司 | Cefprozil compound, and dispersible tablets, dry suspension and preparation method thereof |
CN103524533B (en) * | 2013-10-10 | 2016-01-27 | 珠海金鸿药业股份有限公司 | A kind of cefprozil compound, its dispersible tablet, dry suspensoid and preparation method |
Also Published As
Publication number | Publication date |
---|---|
CA2454078A1 (en) | 2003-02-13 |
TWI250982B (en) | 2006-03-11 |
EP1414827A2 (en) | 2004-05-06 |
GB0118764D0 (en) | 2001-09-26 |
US20040192909A1 (en) | 2004-09-30 |
US7355041B2 (en) | 2008-04-08 |
WO2003011871A3 (en) | 2003-12-04 |
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